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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SAMHD1, TLDC2
(D623G +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
SAMHD1
(R348C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SAMHD1
Single nucleotide variant
(5 prime UTR variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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